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DO Term : progressive supranuclear palsy [DOID:678] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A movement disease that is characterized by serious and progressive problems with control of gait and balance, along with complex eye movement and thinking problems. It involves gradual deterioration and death of specific volumes of the brain.

synonyms:
MESH:D013494,
OMIM:609454,
NCI:C85028,
UMLS_CUI:C0038868,
Steele-Richardson-Olszewski syndrome,
ICD10CM:G23.1,
601104,
OMIM:601104,
610898,
ORDO:683,
GARD:7471,
OMIM:610898,
609454,
progressive supranuclear ophthalmoplegia,
SNOMEDCT_US_2023_03_01:192975003

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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